Canonical Allele Identifier: PA2827998204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2300Ala
CA046787
NM_001354901.2:c.6898T>G